Identity

Trade Name
NAR Kit FDA UDI
Generic Name
Blood collection set, invasive FDA UDI
Device Name
KIT, MODULE, BLOOD SURVEILLANCE FDA UDI
Model / Reference
83-0025 FDA UDI
Description
KIT, MODULE, BLOOD SURVEILLANCE FDA UDI

Identifiers

Catalog Number
83-0025 FDA UDI
Primary DI / UDI-DI
00842209107650 FDA UDI
GMDN Term
Blood collection set, invasive FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood collection set, invasive

NAR Kit by North American Rescue, Llc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection set, invasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cfb8cf5c-2258-4d4f-a774-01a72cb4c8a2 34 fields · synced Jun 1, 2026